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A randomized, double-blinded, parallel-group study in patients with iron deficiency anemia

A Comparative Study of JTT-751 with Sodium Ferrous Citrate in Patients with Iron Deficiency Anemia

Status
Active, not recruiting
Phases
Phase 3
Study type
Interventional
Source
JPRN
Registry ID
JPRN-jRCT2080223942
Enrollment
480
Registered
2018-06-13
Start date
2018-07-03
Completion date
Unknown
Last updated
2026-06-29

For informational purposes only — not medical advice. Sourced from public registries and may not reflect the latest updates. Terms

Conditions

Iron Deficiency Anemia

Interventions

Sponsors

JAPAN TABACCO INC.
Lead Sponsor

Eligibility

Sex/Gender
All

Inclusion criteria

Inclusion criteria: Iron deficiency anemia Hemoglobin level of >= 7.0 g/dL and < 11.0 g/dL

Exclusion criteria

Exclusion criteria: Anemia caused by other than iron deficiency Serum phosphate < 2.5 mg/dL Uncontrollable treatment potentially affecting bleeding in patients with bleeding lesion

Design outcomes

Primary

MeasureTime frame
efficacy Changes in hemoglobin level

Secondary

MeasureTime frame
efficacy Changes in erythrocyte- and iron-related test values

Countries

Japan

Outcome results

None listed

Source: JPRN (via WHO ICTRP) · Data processed: Jul 3, 2026